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U.S. Department of Health and Human Services

Enforcement Report - Week of April 16, 2014

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Product Detail

Product Description Demerol, meperidine HCL Inj. USP, 25 mg/0.5 mL (50 mg/mL), 0.5 mL ampoules, Rx only, NDC 0409-1203-01, Hospira, Inc., Lake Forest, IL.
Recall Number D-1226-2014
Classification Class III
Code Info Lot: 221303A, 1OCT2014
Product Distributed Qty 237,850 ampoules
Reason For Recall Labeling; Missing label; ampoules are missing the immediate container label

Event Detail

Event Id 67750
Product Type Drugs
Status Ongoing
Recalling Firm Hospira Inc.
City Lake Forest
State IL
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2014-03-25
Initial Firm Notification of Consignee or Public Letter
Distribution Pattern Nationwide